Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Victor N. Ortiz-Justiniano"'
Autor:
Karely Correa-Calderas, Ricardo Fraticelli-Rosado, Ashla Gaibi-Rodriguez, Victor N. Ortiz-Justiniano
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 60, Iss , Pp 101555- (2020)
Introduction: The ischiorectal fossa is a fat-containing space around the anal canal. Primary lesions in this area are rare and can present as cystic or solid, and can be benign or malignant. Ischiorectal lipomas are a rare entity with scarce literat
Externí odkaz:
https://doaj.org/article/96aea41308b445c3be84b60134b8faf4
Autor:
Héctor Quintero-Álvarez, MS, Zasha Vázquez-Colón, MD, Victor N. Ortiz-Justiniano, MD, FAPSA, FACS, FAAP
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 29, Iss C, Pp 18-21 (2018)
Arteriovenous malformations (AVMs) are rare lesions that may mimic giant hemangiomas. The most common location is the head and neck region, although very few reports of thoracic AVMs have been described. These lesions grow through childhood and adult
Externí odkaz:
https://doaj.org/article/3c1184d373a442e79572eec077746b5d
Autor:
Omar A. Santiago Báez, Atenas A. Martínez Bernal, Pedro E. Ruiz Medina, Jaime A. Aponte Ortiz, Victor N. Ortiz Justiniano
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 82, Iss , Pp 102302- (2022)
Desmoid tumors are rare, aggressive fibroblastic soft tissue tumors. We report a case of a 20-year-old male with recurrence of desmoid tumor of the left shoulder after initial complete resection 3 years prior. Pathology revealed fibromatosis desmoid
Externí odkaz:
https://doaj.org/article/203151088e9c414fbc26975f232ac9e0
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 82, Iss , Pp 102296- (2022)
Spontaneous jejunal perforation is uncommonly seen in the pediatric population. Many etiologies are implicated, including the rare instance of acute pancreatitis. The digestive pancreatic enzymes cause inflammation, ischemia and necrosis which may le
Externí odkaz:
https://doaj.org/article/c9c33be20e884941a66c9cb109ccffa7
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 71, Iss , Pp 101915- (2021)
Osteogenesis imperfecta is a genetic disorder caused by mutations in genes affecting type I collagen that is mostly found in bone, skin and tendons. In addition to bone fragility and increased risk of fractures, patients with osteogenesis imperfecta
Externí odkaz:
https://doaj.org/article/1fe3bcab059b4506ab13e737facaefd8
Autor:
Nelimar Cruz-Centeno, Jean F. Saenz-Maisonet, Paola M. López-Dones, Alberto Santiago-Cornier, Victor N. Ortiz-Justiniano
Publikováno v:
The American journal of case reports. 23
BACKGROUND Osteogenesis imperfecta is a skeletal disease with a range of phenotypes, depending on the genetic mutation. Individuals with osteogenesis imperfecta type I often have mutations in COL1A genes. This disease can be associated with chest wal
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 29, Iss C, Pp 18-21 (2018)
Arteriovenous malformations (AVMs) are rare lesions that may mimic giant hemangiomas. The most common location is the head and neck region, although very few reports of thoracic AVMs have been described. These lesions grow through childhood and adult
Autor:
Hector Quintero, Victor N. Ortiz Justiniano, Ada L. Rivera Cruz, Cesar Carballo Cuello, Zasha F. Vázquez Colón
Publikováno v:
Open Journal of Pediatrics. :29-33
Background: Necrotizing fasciitis is a soft tissue infection that occurs predominantly in adults. Although rare, only 70 cases have been reported in neonates. This entity, most commonly caused by multiple organisms is often fatal, with 50% mortality.